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9-ethyl-9H-carbazole-3-carboxylic acid phenylethylamide

Base Information Edit
  • Chemical Name:9-ethyl-9H-carbazole-3-carboxylic acid phenylethylamide
  • CAS No.:432506-50-8
  • Molecular Formula:C23H22N2O
  • Molecular Weight:342.44
  • Hs Code.:
  • Mol file:432506-50-8.mol
9-ethyl-9H-carbazole-3-carboxylic acid phenylethylamide

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Chemical Property of 9-ethyl-9H-carbazole-3-carboxylic acid phenylethylamide Edit
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Technology Process of 9-ethyl-9H-carbazole-3-carboxylic acid phenylethylamide

There total 6 articles about 9-ethyl-9H-carbazole-3-carboxylic acid phenylethylamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With dmap; triethylamine; In dichloromethane; at 20 ℃; for 18h;
DOI:10.1071/CH16169
Guidance literature:
Multi-step reaction with 5 steps
1: sodium hydride / N,N-dimethyl-formamide / 18 h / 20 °C
2: titanium tetrachloride / dichloromethane / 4 h / -78 °C
3: potassium permanganate / acetone / 2 h / 20 °C
4: thionyl chloride / 3 h / Reflux
5: triethylamine; dmap / dichloromethane / 18 h / 20 °C
With dmap; potassium permanganate; thionyl chloride; titanium tetrachloride; sodium hydride; triethylamine; In dichloromethane; N,N-dimethyl-formamide; acetone; 2: |Rieche Formylation;
DOI:10.1071/CH16169
Guidance literature:
Multi-step reaction with 4 steps
1: titanium tetrachloride / dichloromethane / 4 h / -78 °C
2: potassium permanganate / acetone / 2 h / 20 °C
3: thionyl chloride / 3 h / Reflux
4: triethylamine; dmap / dichloromethane / 18 h / 20 °C
With dmap; potassium permanganate; thionyl chloride; titanium tetrachloride; triethylamine; In dichloromethane; acetone; 1: |Rieche Formylation;
DOI:10.1071/CH16169
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